由HSV-2感染引起的HLH:一例报告和文献综述。

4区医学 Q3 Medicine

Netherlands Journal of Medicine Pub Date : 2020-09-01

E M Jongbloed, M A W Hermans, M Wabbijn, J J A van Kampen, J A M van Laar

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引用次数: 0

摘要

嗜血球性淋巴组织细胞增多症(HLH)是一种罕见的高炎症性疾病，可由感染、恶性肿瘤或自身免疫性疾病引发。在这里，我们报告了一个由单纯疱疹病毒2型(HSV-2)原发性感染引发的快速进展的HLH患者。患者静脉注射大剂量阿昔洛韦、免疫球蛋白和地塞米松治疗成功。这是在免疫功能正常的成人患者中首次报道hsv -2相关的HLH。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

本刊更多论文

HLH caused by an HSV-2 infection: a case report and review of the literature.

Haemophagocytic lymphohistiocytosis (HLH) is a rare hyperinflammatory condition that can be triggered by infections, malignancies, or auto-immune diseases. Here, we present a patient with rapidly progressive HLH triggered by a herpes simplex virus type 2 (HSV-2) primary infection. The patient was successfully treated with intravenous high-dose acyclovir, immunoglobulins, and dexamethasone. This is the first report of HSV-2-associated HLH in an immunocompetent adult patient.

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来源期刊

Netherlands Journal of Medicine 医学-医学：内科

自引率

0.00%

发文量

审稿时长

6-12 weeks

期刊介绍： The Netherlands Journal of Medicine publishes papers in all relevant fields of internal medicine. In addition to reports of original clinical and experimental studies, reviews on topics of interest or importance, case reports, book reviews and letters to the editor are welcomed.